Product Details

SNP ID

rs61741375

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:168057221 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCTGCCAGCCTGCAGTCCAGGGCG[C/T]GGTGGAAGGTATGGCTGAGTGAGGT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FRMD1 PubMed Links

Gene Details

Gene

FRMD1

Gene Name

FERM domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001122841.2	1441	Missense Mutation	CAC,CGC	H441R	NP_001116313.1
NM_024919.4	1441	Missense Mutation	CAC,CGC	H509R	NP_079195.3
XM_011536137.1	1441	Missense Mutation	CAC,CGC	H574R	XP_011534439.1
XM_011536138.1	1441	Missense Mutation	CAC,CGC	H512R	XP_011534440.1
XM_011536140.1	1441	Missense Mutation	CAC,CGC	H485R	XP_011534442.1
XM_011536141.1	1441	Missense Mutation	CAC,CGC	H466R	XP_011534443.1
XM_011536142.2	1441	Missense Mutation	CAC,CGC	H466R	XP_011534444.1
XM_011536143.1	1441	Missense Mutation	CAC,CGC	H466R	XP_011534445.1
XM_011536145.1	1441	Missense Mutation	CAC,CGC	H464R	XP_011534447.1
XM_011536146.2	1441	Missense Mutation	CAC,CGC	H303R	XP_011534448.1
XM_017011317.1	1441	Missense Mutation	CAC,CGC	H551R	XP_016866806.1
XM_017011318.1	1441	Missense Mutation	CAC,CGC	H303R	XP_016866807.1

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